- CAS 32933-86-1
- Purity 99%
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What is the 3-(2-chloroethyl)-1H-indole ?
3-(2-chloroethyl)-1H-indole is , while it's Molecular Formula is C10H10 Cl N. Used in Pharmaceutical Industry:
3-(2-chloroethyl)-1H-indole is used as a pharmaceutical intermediate for its potential antitumor and cytotoxic effects. It is being studied for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for the development of new anticancer drugs.
Used in Chemical Industry:
3-(2-chloroethyl)-1H-indole is used as a chemical intermediate in the synthesis of other organic compounds. Its unique structure and functional groups allow it to be a key component in the production of various chemical products, contributing to the advancement of the chemical industry.
What is the CAS number for 3-(2-chloroethyl)-1H-indole ?
The CAS number of 3-(2-chloroethyl)-1H-indole is 32933-86-1.
More information of 3-(2-chloroethyl)-1H-indole 32933-86-1 are:
|
Synonyms |
Indole, 3-(2-chloroethyl)- (8CI); 3-(2-Chloroethyl)indole |
|
CAS?Number |
32933-86-1 |
|
Molecular Formula |
C10H10 Cl N |
|
Molecular Weight |
179.649 |
|
Density |
1.229g/cm3 |
|
Boiling Point |
342.4°Cat760mmHg |
|
Flash Point |
191.5°C |
|
HS CODE |
2933990090 |
|
PSA |
15.79000 |
|
LogP |
2.94920 |
What is 3-(2-chloroethyl)-1H-indole (32933-86-1) used for?
3-(2-chloroethyl)-1H-indole is a synthetic chemical compound with the molecular formula C10H10ClN. It is a derivative of the indole family, which is prevalent in various natural products. 3-(2-chloroethyl)-1H-indole features a chlorine atom and an ethyl group attached to the indole ring, endowing it with potential biological activities such as antitumor and cytotoxic effects. It also serves as an intermediate in the synthesis of other organic compounds, making it a versatile chemical with applications in pharmaceutical and chemical industries.
InChI:InChI=1/C10H10ClN/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6H2
Articles related to 3-(2-chloroethyl)-1H-indole:
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Article |
Source |
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Lewis Base Catalysis Enables the Activation of Alcohols by means of Chloroformates as Phosgene Substitutes |
Zoller, Ben,Stach, Tanja,Huy, Peter H. , p. 5637 - 5643 (2020/09/21) |
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METHOD OF CONVERTING ALCOHOL TO HALIDE |
- Page/Page column 51; 172, (2017/01/02) |
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